WO2013108838A1 - Method for producing carrot pectin - Google Patents
Method for producing carrot pectin Download PDFInfo
- Publication number
- WO2013108838A1 WO2013108838A1 PCT/JP2013/050806 JP2013050806W WO2013108838A1 WO 2013108838 A1 WO2013108838 A1 WO 2013108838A1 JP 2013050806 W JP2013050806 W JP 2013050806W WO 2013108838 A1 WO2013108838 A1 WO 2013108838A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- carrot
- pectin
- water
- extraction
- carrot pectin
- Prior art date
Links
- 244000000626 Daucus carota Species 0.000 title claims abstract description 74
- 235000002767 Daucus carota Nutrition 0.000 title claims abstract description 74
- 239000001814 pectin Substances 0.000 title claims abstract description 70
- 235000010987 pectin Nutrition 0.000 title claims abstract description 70
- 229920001277 pectin Polymers 0.000 title claims abstract description 70
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 26
- 239000006185 dispersion Substances 0.000 claims abstract description 41
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 26
- 229910001868 water Inorganic materials 0.000 claims abstract description 26
- 108090000623 proteins and genes Proteins 0.000 claims abstract description 25
- 102000004169 proteins and genes Human genes 0.000 claims abstract description 25
- 238000000605 extraction Methods 0.000 claims description 26
- 235000013305 food Nutrition 0.000 claims description 26
- 101800000263 Acidic protein Proteins 0.000 claims description 23
- 239000003381 stabilizer Substances 0.000 claims description 22
- 239000002994 raw material Substances 0.000 claims description 6
- 238000000034 method Methods 0.000 abstract description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 24
- 230000002378 acidificating effect Effects 0.000 description 9
- 239000002253 acid Substances 0.000 description 8
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 238000005119 centrifugation Methods 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 235000013336 milk Nutrition 0.000 description 6
- 239000008267 milk Substances 0.000 description 6
- 210000004080 milk Anatomy 0.000 description 6
- 235000020124 milk-based beverage Nutrition 0.000 description 6
- 238000005063 solubilization Methods 0.000 description 5
- 108010082495 Dietary Plant Proteins Proteins 0.000 description 4
- 235000010469 Glycine max Nutrition 0.000 description 4
- 244000068988 Glycine max Species 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 241001465754 Metazoa Species 0.000 description 4
- 235000015190 carrot juice Nutrition 0.000 description 4
- -1 cation carbonate Chemical class 0.000 description 4
- 235000015140 cultured milk Nutrition 0.000 description 4
- 238000012869 ethanol precipitation Methods 0.000 description 4
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 4
- 238000001556 precipitation Methods 0.000 description 4
- 238000000926 separation method Methods 0.000 description 4
- PYMYPHUHKUWMLA-UHFFFAOYSA-N 2,3,4,5-tetrahydroxypentanal Chemical compound OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 241000894006 Bacteria Species 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 235000011850 desserts Nutrition 0.000 description 3
- 150000004676 glycans Chemical class 0.000 description 3
- 239000004310 lactic acid Substances 0.000 description 3
- 235000014655 lactic acid Nutrition 0.000 description 3
- 229920001282 polysaccharide Polymers 0.000 description 3
- 239000005017 polysaccharide Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 235000013322 soy milk Nutrition 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 241000207199 Citrus Species 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 239000000872 buffer Substances 0.000 description 2
- 239000007853 buffer solution Substances 0.000 description 2
- 235000015165 citric acid Nutrition 0.000 description 2
- 235000020971 citrus fruits Nutrition 0.000 description 2
- 229940040387 citrus pectin Drugs 0.000 description 2
- 239000009194 citrus pectin Substances 0.000 description 2
- 235000013353 coffee beverage Nutrition 0.000 description 2
- 230000032050 esterification Effects 0.000 description 2
- 238000005886 esterification reaction Methods 0.000 description 2
- 235000015203 fruit juice Nutrition 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 235000020183 skimmed milk Nutrition 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000006228 supernatant Substances 0.000 description 2
- 235000015192 vegetable juice Nutrition 0.000 description 2
- 235000013311 vegetables Nutrition 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229920001661 Chitosan Polymers 0.000 description 1
- 235000019750 Crude protein Nutrition 0.000 description 1
- AEMOLEFTQBMNLQ-YMDCURPLSA-N D-galactopyranuronic acid Chemical compound OC1O[C@H](C(O)=O)[C@H](O)[C@H](O)[C@H]1O AEMOLEFTQBMNLQ-YMDCURPLSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- IAJILQKETJEXLJ-UHFFFAOYSA-N Galacturonsaeure Natural products O=CC(O)C(O)C(O)C(O)C(O)=O IAJILQKETJEXLJ-UHFFFAOYSA-N 0.000 description 1
- IMQLKJBTEOYOSI-GPIVLXJGSA-N Inositol-hexakisphosphate Chemical compound OP(O)(=O)O[C@H]1[C@H](OP(O)(O)=O)[C@@H](OP(O)(O)=O)[C@H](OP(O)(O)=O)[C@H](OP(O)(O)=O)[C@@H]1OP(O)(O)=O IMQLKJBTEOYOSI-GPIVLXJGSA-N 0.000 description 1
- 238000007696 Kjeldahl method Methods 0.000 description 1
- 229920000168 Microcrystalline cellulose Polymers 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- IMQLKJBTEOYOSI-UHFFFAOYSA-N Phytic acid Natural products OP(O)(=O)OC1C(OP(O)(O)=O)C(OP(O)(O)=O)C(OP(O)(O)=O)C(OP(O)(O)=O)C1OP(O)(O)=O IMQLKJBTEOYOSI-UHFFFAOYSA-N 0.000 description 1
- HDSBZMRLPLPFLQ-UHFFFAOYSA-N Propylene glycol alginate Chemical compound OC1C(O)C(OC)OC(C(O)=O)C1OC1C(O)C(O)C(C)C(C(=O)OCC(C)O)O1 HDSBZMRLPLPFLQ-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 235000010724 Wisteria floribunda Nutrition 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 238000004380 ashing Methods 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 235000014633 carbohydrates Nutrition 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010418 carrageenan Nutrition 0.000 description 1
- 239000000679 carrageenan Substances 0.000 description 1
- 229920001525 carrageenan Polymers 0.000 description 1
- 229940113118 carrageenan Drugs 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 238000004737 colorimetric analysis Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 235000013365 dairy product Nutrition 0.000 description 1
- 238000000909 electrodialysis Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 235000013861 fat-free Nutrition 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 235000020251 goat milk Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 235000015243 ice cream Nutrition 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000003456 ion exchange resin Substances 0.000 description 1
- 229920003303 ion-exchange polymer Polymers 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 235000019813 microcrystalline cellulose Nutrition 0.000 description 1
- 239000008108 microcrystalline cellulose Substances 0.000 description 1
- 229940016286 microcrystalline cellulose Drugs 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- OQUKIQWCVTZJAF-UHFFFAOYSA-N phenol;sulfuric acid Chemical compound OS(O)(=O)=O.OC1=CC=CC=C1 OQUKIQWCVTZJAF-UHFFFAOYSA-N 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 235000014786 phosphorus Nutrition 0.000 description 1
- 235000002949 phytic acid Nutrition 0.000 description 1
- 239000000467 phytic acid Substances 0.000 description 1
- 229940068041 phytic acid Drugs 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 239000000770 propane-1,2-diol alginate Substances 0.000 description 1
- 235000010409 propane-1,2-diol alginate Nutrition 0.000 description 1
- 235000021568 protein beverage Nutrition 0.000 description 1
- 235000011962 puddings Nutrition 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 230000009291 secondary effect Effects 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- 230000007928 solubilization Effects 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 235000008939 whole milk Nutrition 0.000 description 1
- 235000013618 yogurt Nutrition 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B37/00—Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
- C08B37/0003—General processes for their isolation or fractionation, e.g. purification or extraction from biomass
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23C—DAIRY PRODUCTS, e.g. MILK, BUTTER OR CHEESE; MILK OR CHEESE SUBSTITUTES; MAKING THEREOF
- A23C9/00—Milk preparations; Milk powder or milk powder preparations
- A23C9/152—Milk preparations; Milk powder or milk powder preparations containing additives
- A23C9/154—Milk preparations; Milk powder or milk powder preparations containing additives containing thickening substances, eggs or cereal preparations; Milk gels
- A23C9/1542—Acidified milk products containing thickening agents or acidified milk gels, e.g. acidified by fruit juices
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
- A23L2/52—Adding ingredients
- A23L2/62—Clouding agents; Agents to improve the cloud-stability
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L29/00—Foods or foodstuffs containing additives; Preparation or treatment thereof
- A23L29/20—Foods or foodstuffs containing additives; Preparation or treatment thereof containing gelling or thickening agents
- A23L29/206—Foods or foodstuffs containing additives; Preparation or treatment thereof containing gelling or thickening agents of vegetable origin
- A23L29/231—Pectin; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B37/00—Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
- C08B37/0006—Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid
- C08B37/0045—Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid alpha-D-Galacturonans, e.g. methyl ester of (alpha-1,4)-linked D-galacturonic acid units, i.e. pectin, or hydrolysis product of methyl ester of alpha-1,4-linked D-galacturonic acid units, i.e. pectinic acid; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
Definitions
- the present invention relates to a method for producing carrot pectin.
- the present invention also relates to a dispersion stabilizer for acidic protein foods. Furthermore, this invention relates to an acidic protein foodstuff and its manufacturing method.
- Patent Document 1 pectin extracted from root vegetables with hot water at 100 ° C. or higher under acidic conditions serves as a stabilizer for acidic protein foods.
- the carrot pectin extracted with hot water of 100 ° C. or higher exhibits sufficient dispersion stability for proteins only in a narrow range of pH 4.2 to 4.4. They found out. If the dispersion stability with respect to protein is shown only in a narrow pH range, foods to which carrot pectin can be applied are limited, which is not preferable. Then, it aims at providing the carrot pectin which shows the outstanding dispersion stability with respect to protein in a wide pH range.
- carrot pectin extracted under a predetermined pH condition with water having a temperature of less than 100 ° C. exhibits excellent dispersion stability with respect to proteins in a wide pH range, thereby completing the present invention. It was.
- the present invention relates to a method for producing carrot pectin, in which carrot is extracted with water having a temperature of less than 100 ° C. under conditions of pH 2 or more and 5 or less.
- Carrot pectin obtained by this production method exhibits excellent dispersion stability for proteins in a wide pH range.
- Carrot juice residue is produced in large quantities in the process of producing vegetable juice made from carrots on an industrial scale, and is usually treated as waste.
- secondary effects such as reduction in vegetable juice production cost and environmental impact can be expected.
- the temperature of the water to be extracted is preferably 60 ° C. or higher and 90 ° C. or lower.
- extraction is preferably performed under conditions of pH 2.5 or more and 4.5 or less. By extracting under these conditions, it is possible to produce carrot pectin that exhibits excellent dispersion stability for proteins in a wider pH range.
- the present invention also relates to a dispersion stabilizer for acidic protein foods containing carrot pectin obtained by the above production method. It utilizes the excellent dispersion stability of carrot pectin obtained by the above production method with respect to protein.
- the above dispersion stabilizer can disperse and stabilize proteins under conditions of pH 4 or more and 4.6 or less. It exhibits dispersion stability for proteins in a wider pH range than the dispersion stabilizers obtained by conventional methods.
- the present invention further relates to a method for producing an acidic protein food to which the dispersion stabilizer is added and an acidic protein food to which the dispersion stabilizer is added.
- the carrot pectin obtained by the production method of the present invention exhibits excellent dispersion stability for proteins in a wide pH range.
- the carrot used as a raw material may be the whole carrot root or a juice residue.
- the squeezed residue may be frozen or lyophilized. From the viewpoint of effective use of resources and from the viewpoint of ease of extraction work, it is preferable to use juice residue as a raw material.
- the method for producing carrot pectin of the present invention comprises a step of extracting carrot with water at a temperature of less than 100 ° C. under conditions of pH 2 or more and 5 or less. By extracting under such conditions, carrot pectin exhibiting excellent dispersion stability for proteins in a wide pH range can be obtained.
- the pH is adjusted with mineral acids such as hydrochloric acid, sulfuric acid and phosphoric acid, organic acids such as citric acid, oxalic acid, tartaric acid and acetic acid, alkali metal such as sodium hydroxide and calcium hydroxide, and water of divalent cation.
- An oxide, an alkali metal, a divalent cation carbonate, a hydrogen carbonate, or the like can be used.
- the yield of carrot pectin may be improved by adding a substance having a chelating function such as hexametaphosphoric acid, phytic acid or EDTA.
- the extraction temperature is not particularly limited as long as it is lower than 100 ° C, but it is preferably 60 ° C or higher and 90 ° C or lower in consideration of yield and hygiene.
- the extraction temperature is low, the extraction time tends to be long, and when the extraction temperature is high, the dispersion stability of the carrot pectin obtained to the protein tends to decrease.
- the extraction pH may be 2 or more and 5 or less, preferably 2.5 or more and 4.5 or less, and more preferably 2.5 or more and 4 or less. If the extraction pH is too low or too high, the dispersion stability of the carrot pectin obtained to the protein tends to decrease.
- Preferred combinations of extraction temperature and pH for improving the dispersion stability of the obtained carrot pectin with respect to protein include 60 ° C. or higher and 90 ° C. or lower and pH 2.5 or higher and 4.5 or lower. Of 60 ° C. or more and 90 ° C. or less and pH 2.5 or more and 4 or less. Another preferable combination includes 60 ° C. or higher and 80 ° C. or lower and pH 2 or higher and 4.5 or lower, and another more preferable combination includes 60 ° C. or higher and 80 ° C. or lower and pH 2 or higher and 4 or lower.
- the mixing ratio of carrot and water or buffer is not particularly limited, but from the viewpoint of ease of operation after extraction and yield, 5 to 50 weight of water or buffer with respect to 1 part by weight of carrot in terms of dry matter.
- the amount is preferably 10 to 30 parts by weight of water or a buffer solution with respect to 1 part by weight of carrot.
- the mixture is solid-liquid separated by a method such as centrifugation or filter press. Insoluble components are separated as a solid, while carrot pectin is contained in the water-soluble fraction.
- the separated supernatant can be dried and used as it is, but the use of pectin is more valuable.
- any method for separating and removing components other than pectin such as mixed pigment components, proteins, and ash can be used.
- activated carbon, electrodialysis, ion exchange resin, hydrophobic resin, UF membrane, or a hydrophilic polar solvent such as ethanol or isopropanol can be used alone or in combination.
- an ethanol precipitation method that can purify carrot pectin by using the property of precipitating carrot pectin by adding ethanol is effective.
- the ethanol precipitation operation may be performed once, but it is preferably performed twice in order to increase the purity of carrot pectin.
- the second ethanol concentration is preferably higher than the first ethanol concentration. More specifically, for example, ethanol is added to the separated supernatant to precipitate carrot pectin. The amount of ethanol added is such that the final concentration in the system is 50 to 70% by weight, preferably 60% by weight.
- the precipitated pectin is subjected to solid-liquid separation by centrifugation or standing.
- the collected pectin is washed with water-containing ethanol.
- the water-containing ethanol used for washing is water-containing ethanol containing 70 to 90% by weight, preferably 80% by weight ethanol. After washing, solid-liquid separation is performed again by centrifugation or standing.
- the dispersion stabilizer for acidic protein foods of the present invention contains carrot pectin obtained by the method for producing carrot pectin.
- Acidic protein foods are acidic foods that contain animal and vegetable proteins, and drinks that use animal and vegetable proteins such as milk and soy milk, citrus juice or other juices, or organic acids or phosphorus such as citric acid and lactic acid.
- Acidic protein beverages made by adding inorganic acids such as acids, acidic milk beverages made from dairy products made acidic, iced ice cream and other frozen desserts containing fruit juice, acid frozen desserts such as frozen yogurt, pudding Includes acidified desserts and coffee drinks, fruit juices added to gelled foods such as bavaroa, coffee drinks, lactic acid bacteria drinks (including live bacteria and bactericidal types), fermented milk (solid or liquid), and other acid protein foods To do.
- Animal and vegetable proteins are milk, goat milk, skim milk, soy milk, powdered whole milk powder, skim milk powder, powdered soy milk, sweetened milk added with sugar, concentrated concentrated milk, minerals such as calcium, etc.
- fermented milk refers to the fermented milk fermented by adding the lactic acid bacteria starter after sterilizing the said animal and vegetable protein, it may be further pulverized or added with sugar or the like as desired.
- the dispersion stabilizer refers to a substance having a function of allowing the protein to be uniformly dispersed without being precipitated in the food by being added to the acidic protein food.
- the amount of the dispersion stabilizer added to the acidic protein food is not particularly limited, but is preferably 0.05 to 10% by weight, more preferably carrot pectin with respect to the final product in order to exhibit sufficient dispersion stability. Is added so as to contain 0.2 to 5% by weight.
- the dispersion stabilizer for acidic protein food of the present invention can disperse and stabilize proteins in a wide pH range of pH 4 or more and 4.6 or less.
- the dispersion stabilizer for acidic protein foods of the present invention includes conventionally known stabilizers such as pectin derived from apple or citrus, water-soluble soybean polysaccharide, sodium carboxymethylcellulose, propylene glycol alginate, carrageenan
- pectin derived from apple or citrus water-soluble soybean polysaccharide
- sodium carboxymethylcellulose propylene glycol alginate
- carrageenan microcrystalline cellulose, chitosan, organic acid salt, polymerized phosphate, emulsifier, heat-denatured protein, and the like may be contained, and thereby, the expansion of the pH range showing the dispersion stability to the protein can be achieved.
- the dispersion stabilizer is added to the acidic protein food of the present invention. Moreover, the manufacturing method of the acidic protein foodstuff of this invention is equipped with the process which the said dispersion stabilizer adds. By adding the above-mentioned dispersion stabilizer, it is possible to uniformly disperse the protein in the acidic protein food, thereby providing a good appearance and flavor and increasing the commercial value. it can.
- acidic protein foods and the amount of dispersion stabilizer added to acidic protein foods are as described above.
- Example 1 Extraction of carrot pectin with hot water at 80 ° C
- Carrot juice residue (hereinafter also referred to as carrot pulp) was lyophilized as a raw material, and carrots under hot water at 80 ° C and pH 2-6 Pectin was extracted.
- 95 parts by weight of water was added to 5 parts by weight of lyophilized carrot pulp, and the pH was adjusted to 2-6 using hydrochloric acid or an aqueous sodium hydroxide solution. After heating at 80 ° C. for 120 minutes, solid-liquid separation was performed by centrifugation (8000 rpm, 30 minutes) into an insoluble component and a water-soluble pectin-containing fraction.
- Pectin was precipitated by adding ethanol to the pectin-containing fraction to a final concentration of 60% by weight. The precipitated pectin was recovered by centrifugation (8000 rpm, 30 minutes). The recovered pectin was washed with 80% by weight of water-containing ethanol, and pectin was recovered again by centrifugation (8000 rpm, 30 minutes). The collected pectin was air-dried to obtain carrot pectin.
- the water-soluble rate of carrot pectin was calculated by dividing the dry matter amount of the water-soluble pectin-containing fraction at the time of the first solid-liquid separation by the dry matter amount in the slurry before extraction.
- the yield was calculated by dividing the dry weight of the carrot pectin finally obtained by the dry weight of carrot pulp.
- the water-solubilization rate and yield under each condition are summarized in Table 1.
- the analytical values of the carrot pectin obtained are also summarized in Table 1.
- the total amount of sugar was calculated by the phenol-sulfuric acid method, the amount of reducing sugar was calculated by the Somogyi-Nelson method, the amount of uronic acid was calculated by the Blumenklantz method, and the amount of starch was calculated by the iodine colorimetric method.
- the degree of methyl esterification was calculated by the official method (titration method) of pectin.
- the crude protein was calculated by the Kjeldahl method, and the ash content was calculated by the ashing method.
- the extracted carrot pectin is mainly composed of carbohydrates, has a high galacturonic acid content of 45% or more, and has a methyl esterification degree of 60% or more and high methoxyl pectin. It was confirmed that there was.
- Example 2 Extraction of carrot pectin with hot water at 60 ° C
- carrot pectin was extracted from carrot pulp.
- the extraction temperature was 60 ° C. Table 2 summarizes the water-solubilization rate, yield, and various analytical values under each condition.
- Example 3 Extraction of carrot pectin with hot water at 90 ° C
- carrot pectin was extracted from carrot pulp.
- the extraction temperature was 90 ° C.
- Table 3 summarizes the water solubility, yield, and various analytical values under each condition.
- the water-solubilization rate exceeded 72%, and the hydrolysis more than necessary of pectin was estimated.
- Comparative Example 1 Extraction of carrot pectin with pressurized hot water at 100 ° C. or higher
- carrot pectin was extracted from carrot pulp.
- extraction temperature was 105 degreeC or 120 degreeC.
- Table 4 summarizes the water-solubilization rate, yield, and various analytical values under each condition.
- Test Example 1 Dispersion Stabilization of Acidic Milk Beverage
- the dispersion stability of carrot pectin obtained in Examples 1 to 3 and Comparative Example 1 with respect to acidic protein foods was evaluated.
- the pH of the acidic milk beverage (non-fat milk solid content: 3.0%) was changed in the range of 3.8 to 4.8, and the precipitation rate when 0.2% by weight of carrot pectin was added was examined.
- the precipitation rate is 2% or less, it is stable ( ⁇ ), when the precipitation rate is over 2% and 5% or less, it is metastable ( ⁇ ), and when the precipitation rate is over 5%, there is no stability ( ⁇ ).
- Tables 5 to 8 summarize the results.
- carrot pectin, water-soluble soybean polysaccharide and citrus pectin extracted at a temperature exceeding 100 ° C. did not show sufficient dispersion stability in an acidic milk beverage at pH 4.6.
- carrot pectin extracted under conditions of 60 ° C. or higher and lower than 100 ° C. and pH 2 or higher and 5 or lower showed dispersion stability with respect to acidic milk beverages in a wide range of pH 4.2 or higher and 4.6 or lower.
- the carrot pectin extracted under conditions of 60 ° C. or higher and lower than 100 ° C. and pH 2 or higher and 4 or lower showed dispersion stability with respect to acidic milk drinks in a wider range of pH 4 or higher and 4.6 or lower.
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Abstract
Description
原料とするニンジンは、ニンジンの根全体であってもよく、搾汁残渣であってもよい。搾汁残渣は凍結や凍結乾燥されたものであってもよい。資源の有効活用という観点から、また、抽出作業の容易さの観点から、搾汁残渣を原料とすることが好ましい。 [Method for producing carrot pectin]
The carrot used as a raw material may be the whole carrot root or a juice residue. The squeezed residue may be frozen or lyophilized. From the viewpoint of effective use of resources and from the viewpoint of ease of extraction work, it is preferable to use juice residue as a raw material.
本発明の酸性タンパク質食品用分散安定化剤は、上記ニンジンペクチンの製造方法で得られるニンジンペクチンを含む。 [Dispersion stabilizer for acidic protein foods]
The dispersion stabilizer for acidic protein foods of the present invention contains carrot pectin obtained by the method for producing carrot pectin.
本発明の酸性タンパク質食品は、上記分散安定化剤が添加されている。また、本発明の酸性タンパク質食品の製造方法は、上記分散安定化剤が添加する工程を備えている。上記分散安定化剤が添加されていることにより、酸性タンパク質食品中にタンパク質が均一に分散することが可能であり、それによって良好な外観や風味を提供することができ、商品価値を高めることができる。 [Acid protein food and production method thereof]
The dispersion stabilizer is added to the acidic protein food of the present invention. Moreover, the manufacturing method of the acidic protein foodstuff of this invention is equipped with the process which the said dispersion stabilizer adds. By adding the above-mentioned dispersion stabilizer, it is possible to uniformly disperse the protein in the acidic protein food, thereby providing a good appearance and flavor and increasing the commercial value. it can.
ニンジン搾汁残渣(以下、ニンジンパルプとも言う)を凍結乾燥したものを原料として用い、80℃の熱水でpH2~6の条件下でニンジンペクチンを抽出した。まず、凍結乾燥したニンジンパルプ5重量部に水95重量部を加え、塩酸又は水酸化ナトリウム水溶液を用いて、pHを2~6に調整した。80℃にて120分間加熱した後、遠心分離(8000rpm、30分間)により、不溶性成分と水溶性のペクチン含有画分とに固液分離した。ペクチン含有画分に最終濃度が60重量%となるようにエタノールを加えることによりペクチンを沈殿させた。沈殿したペクチンを遠心分離(8000rpm、30分間)により回収した。回収したペクチンを80重量%の含水エタノールで洗浄し、再度遠心分離(8000rpm、30分間)によりペクチンを回収した。回収したペクチンを風乾し、ニンジンペクチンを得た。 Example 1: Extraction of carrot pectin with hot water at 80 ° C Carrot juice residue (hereinafter also referred to as carrot pulp) was lyophilized as a raw material, and carrots under hot water at 80 ° C and pH 2-6 Pectin was extracted. First, 95 parts by weight of water was added to 5 parts by weight of lyophilized carrot pulp, and the pH was adjusted to 2-6 using hydrochloric acid or an aqueous sodium hydroxide solution. After heating at 80 ° C. for 120 minutes, solid-liquid separation was performed by centrifugation (8000 rpm, 30 minutes) into an insoluble component and a water-soluble pectin-containing fraction. Pectin was precipitated by adding ethanol to the pectin-containing fraction to a final concentration of 60% by weight. The precipitated pectin was recovered by centrifugation (8000 rpm, 30 minutes). The recovered pectin was washed with 80% by weight of water-containing ethanol, and pectin was recovered again by centrifugation (8000 rpm, 30 minutes). The collected pectin was air-dried to obtain carrot pectin.
実施例1と同様に、ニンジンパルプからニンジンペクチンを抽出した。ただし、抽出温度は60℃とした。各条件における水溶化率、収率及び各種分析値を表2にまとめた。 Example 2: Extraction of carrot pectin with hot water at 60 ° C In the same manner as in Example 1, carrot pectin was extracted from carrot pulp. However, the extraction temperature was 60 ° C. Table 2 summarizes the water-solubilization rate, yield, and various analytical values under each condition.
実施例1と同様に、ニンジンパルプからニンジンペクチンを抽出した。ただし、抽出温度は90℃とした。各条件における水溶化率、収率及び各種分析値を表3にまとめた。尚、抽出pH2.0では、水溶化率が72%を超えており、ペクチンの必要以上の加水分解が推定された。 Example 3: Extraction of carrot pectin with hot water at 90 ° C In the same manner as in Example 1, carrot pectin was extracted from carrot pulp. However, the extraction temperature was 90 ° C. Table 3 summarizes the water solubility, yield, and various analytical values under each condition. In addition, in extraction pH 2.0, the water-solubilization rate exceeded 72%, and the hydrolysis more than necessary of pectin was estimated.
実施例1と同様に、ニンジンパルプからニンジンペクチンを抽出した。ただし、抽出温度は105℃又は120℃とした。各条件における水溶化率、収率及び各種分析値を表4にまとめた。 Comparative Example 1: Extraction of carrot pectin with pressurized hot water at 100 ° C. or higher In the same manner as in Example 1, carrot pectin was extracted from carrot pulp. However, extraction temperature was 105 degreeC or 120 degreeC. Table 4 summarizes the water-solubilization rate, yield, and various analytical values under each condition.
実施例1から3及び比較例1で得られたニンジンペクチンの酸性タンパク質食品に対する分散安定性を評価した。酸性乳飲料(無脂乳固形分3.0%)のpHを3.8~4.8の範囲で変化させ、ニンジンペクチンを0.2重量%添加したときの沈殿率を調べた。沈殿率が2%以下の場合は安定(○)、沈殿率が2%を超えて5%以下の場合は準安定(△)、沈殿率が5%を超えた場合は安定性なし(×)として、表5から8に結果をまとめた。なお、比較対照として酸性乳飲料の分散安定剤として機能することが知られている水溶性大豆多糖類(不二製油株式会社;ソヤファイブ-S-ZR100)及び柑橘ペクチン(三栄源エフ・エフ・アイ株式会社;SM-666)を用いた。 Test Example 1: Dispersion Stabilization of Acidic Milk Beverage The dispersion stability of carrot pectin obtained in Examples 1 to 3 and Comparative Example 1 with respect to acidic protein foods was evaluated. The pH of the acidic milk beverage (non-fat milk solid content: 3.0%) was changed in the range of 3.8 to 4.8, and the precipitation rate when 0.2% by weight of carrot pectin was added was examined. When the precipitation rate is 2% or less, it is stable (○), when the precipitation rate is over 2% and 5% or less, it is metastable (△), and when the precipitation rate is over 5%, there is no stability (×). Tables 5 to 8 summarize the results. As comparative controls, water-soluble soybean polysaccharides (Fuji Oil Co., Ltd .; Soya Five-S-ZR100) and citrus pectin (San-Eigen F.F. Co., Ltd .; SM-666) was used.
Claims (8)
- ニンジンを100℃未満の温度の水でpH2以上5以下の条件下で抽出する、ニンジンペクチンの製造方法。 A method for producing carrot pectin, in which carrot is extracted with water at a temperature of less than 100 ° C. under conditions of pH 2 to 5.
- ニンジンの搾汁残渣を原料として使用する、請求項1記載の製造方法。 The manufacturing method of Claim 1 which uses the squeezed residue of a carrot as a raw material.
- 抽出する水の温度が60°以上90℃以下である、請求項1又は2記載の製造方法。 The manufacturing method according to claim 1 or 2, wherein the temperature of the water to be extracted is 60 ° C or higher and 90 ° C or lower.
- pH2.5以上4.5以下の条件下で抽出する、請求項1~3のいずれか一項記載の製造方法。 The production method according to any one of claims 1 to 3, wherein the extraction is performed under conditions of pH 2.5 to 4.5.
- 請求項1~4のいずれか一項記載の製造方法で得られるニンジンペクチンを含む、酸性タンパク質食品用分散安定化剤。 A dispersion stabilizer for acidic protein foods, comprising carrot pectin obtained by the production method according to any one of claims 1 to 4.
- pH4以上4.6以下の条件下でタンパク質を分散安定化できる、請求項5記載の分散安定化剤。 6. The dispersion stabilizer according to claim 5, wherein the protein can be dispersed and stabilized under conditions of pH 4 or more and 4.6 or less.
- 請求項5又は6記載の分散安定化剤を添加する、酸性タンパク質食品の製造方法。 A method for producing an acidic protein food, wherein the dispersion stabilizer according to claim 5 or 6 is added.
- 請求項5又は6記載の分散安定化剤が添加された、酸性タンパク質食品。 An acidic protein food to which the dispersion stabilizer according to claim 5 or 6 is added.
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BR112014017715A BR112014017715A8 (en) | 2012-01-18 | 2013-01-17 | METHOD FOR THE PRODUCTION OF CARROT PECTIN |
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2013
- 2013-01-17 US US14/372,654 patent/US20150017316A1/en not_active Abandoned
- 2013-01-17 JP JP2013554341A patent/JPWO2013108838A1/en active Pending
- 2013-01-17 WO PCT/JP2013/050806 patent/WO2013108838A1/en active Application Filing
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Cited By (4)
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JP6187669B1 (en) * | 2016-11-28 | 2017-08-30 | 不二製油グループ本社株式会社 | Water-soluble polysaccharides derived from root vegetables and method for producing the same |
WO2018097247A1 (en) * | 2016-11-28 | 2018-05-31 | 不二製油グループ本社株式会社 | Water-soluble polysaccharide derived from root vegetable and method for producing same |
JP2018087264A (en) * | 2016-11-28 | 2018-06-07 | 不二製油グループ本社株式会社 | Water-soluble polysaccharides derived from root crops and method for producing the same |
US11213057B2 (en) | 2016-11-28 | 2022-01-04 | Fuji Oil Holdings Inc. | Water-soluble polysaccharide derived from root vegetable and method for producing same |
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US20150017316A1 (en) | 2015-01-15 |
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JPWO2013108838A1 (en) | 2015-05-11 |
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